McGovern Institute for Brain Research, MIT, 43 Vassar Street, Building 46-6133, Cambridge, MA, USA.
Hum Mol Genet. 2010 May 1;19(9):1756-65. doi: 10.1093/hmg/ddq055. Epub 2010 Feb 10.
Huntingtin protein (Htt) is ubiquitously expressed, yet Huntington's disease (HD), a fatal neurologic disorder produced by expansion of an Htt polyglutamine tract, is characterized by neurodegeneration that occurs primarily in the striatum and cerebral cortex. Such discrepancies between sites of expression and pathology occur in multiple neurodegenerative disorders associated with expanded polyglutamine tracts. One possible reason is that disease-modifying factors are tissue-specific. Here, we show that the striatum-enriched protein, CalDAG-GEFI, is severely down-regulated in the striatum of mouse HD models and is down-regulated in HD individuals. In the R6/2 transgenic mouse model of HD, striatal neurons with the largest aggregates of mutant Htt have the lowest levels of CalDAG-GEFI. In a brain-slice explant model of HD, knock-down of CalDAG-GEFI expression rescues striatal neurons from pathology induced by transfection of polyglutamine-expanded Htt exon 1. These findings suggest that the striking down-regulation of CalDAG-GEFI in HD could be a protective mechanism that mitigates Htt-induced degeneration.
亨廷顿蛋白(Htt)广泛表达,但亨廷顿病(HD)是一种由 Htt 多聚谷氨酰胺片段扩展引起的致命神经退行性疾病,其特征是主要发生在纹状体和大脑皮层的神经退行性变。在与多聚谷氨酰胺片段扩展相关的多种神经退行性疾病中,存在着表达部位与病理学之间的这种差异。一个可能的原因是疾病修饰因子是组织特异性的。在这里,我们表明富含纹状体的蛋白 CalDAG-GEFI 在小鼠 HD 模型的纹状体中严重下调,并且在 HD 个体中下调。在 R6/2 转基因 HD 小鼠模型中,具有最大突变 Htt 聚集体的纹状体神经元中 CalDAG-GEFI 的水平最低。在 HD 的脑切片外植体模型中,CalDAG-GEFI 表达的敲低可挽救由转染多聚谷氨酰胺扩展的 Htt 外显子 1 引起的纹状体神经元的病理。这些发现表明,HD 中 CalDAG-GEFI 的显著下调可能是一种保护机制,可以减轻 Htt 诱导的变性。